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7. De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III). Hayasaka K; Himoro M; Sawaishi Y; Nanao K; Takahashi T; Takada G; Nicholson GA; Ouvrier RA; Tachi N Nat Genet; 1993 Nov; 5(3):266-8. PubMed ID: 7506095 [TBL] [Abstract][Full Text] [Related]
8. Facial nerve dysfunction in hereditary motor and sensory neuropathy type I and III. Glocker FX; Rösler KM; Linden D; Heinen F; Hess CW; Lücking CH Muscle Nerve; 1999 Sep; 22(9):1201-8. PubMed ID: 10454715 [TBL] [Abstract][Full Text] [Related]
9. Germline mosaicism of MPZ gene in Dejerine-Sottas syndrome (HMSN III) associated with hereditary stomatocytosis. Takashima H; Nakagawa M; Kanzaki A; Yawata Y; Horikiri T; Matsuzaki T; Suehara M; Izumo S; Osame M Neuromuscul Disord; 1999 Jun; 9(4):232-8. PubMed ID: 10399750 [TBL] [Abstract][Full Text] [Related]
10. Recessive inheritance of a new point mutation of the PMP22 gene in Dejerine-Sottas disease. Parman Y; Planté-Bordeneuve V; Guiochon-Mantel A; Eraksoy M; Said G Ann Neurol; 1999 Apr; 45(4):518-22. PubMed ID: 10211478 [TBL] [Abstract][Full Text] [Related]
11. Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene. Roa BB; Dyck PJ; Marks HG; Chance PF; Lupski JR Nat Genet; 1993 Nov; 5(3):269-73. PubMed ID: 8275092 [TBL] [Abstract][Full Text] [Related]
12. Hereditary motor and sensory neuropathy type I and type II. Sghirlanzoni A; Pareyson D; Scaioli V; Marazzi R; Pacini L Ital J Neurol Sci; 1990 Oct; 11(5):471-9. PubMed ID: 2272782 [TBL] [Abstract][Full Text] [Related]
13. A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine-Sottas syndrome patients. Silander K; Meretoja P; Nelis E; Timmerman V; Van Broeckhoven C; Aula P; Savontaus ML Hum Mutat; 1996; 8(4):304-10. PubMed ID: 8956034 [TBL] [Abstract][Full Text] [Related]
14. Hereditary demyelinating motor and sensory neuropathy. Gabreëls-Festen A; Gabreëls F Brain Pathol; 1993 Apr; 3(2):135-46. PubMed ID: 8293175 [TBL] [Abstract][Full Text] [Related]
15. X-linked dominant hereditary motor and sensory neuropathy. Hahn AF; Brown WF; Koopman WJ; Feasby TE Brain; 1990 Oct; 113 ( Pt 5)():1511-25. PubMed ID: 2245309 [TBL] [Abstract][Full Text] [Related]
16. Phe 84 deletion of the PMP22 gene associated with hereditary motor and sensory neuropathy HMSN III with multiple cranial neuropathy: clinical, neurophysiological and magnetic resonance imaging findings. Yener GG; Guiochon-Mantel A; Obuz F; Baklan B; Oztürk V; Kovanlikaya I; Cakmur R; Genç A J Neurol; 2001 Mar; 248(3):193-6. PubMed ID: 11355152 [TBL] [Abstract][Full Text] [Related]
17. Hereditary motor and sensory neuropathy: HMSN type II (neuronal type) and X-linked HMSN. Hahn AF Brain Pathol; 1993 Apr; 3(2):147-55. PubMed ID: 8293176 [TBL] [Abstract][Full Text] [Related]
18. Hereditary motor and sensory neuropathy of neuronal type with onset in early childhood. Gabreëls-Festen AA; Joosten EM; Gabreëls FJ; Jennekens FG; Gooskens RH; Stegeman DF Brain; 1991 Aug; 114 ( Pt 4)():1855-70. PubMed ID: 1884182 [TBL] [Abstract][Full Text] [Related]
19. Hereditary motor and sensory neuropathy with calf muscle enlargement. Sakashita Y; Sakato S; Komai K; Takamori M J Neurol Sci; 1992 Nov; 113(1):118-22. PubMed ID: 1469450 [TBL] [Abstract][Full Text] [Related]
20. A Dejerine-Sottas neuropathy family with a gene mapped on chromosome 8. Ionasescu VV; Kimura J; Searby CC; Smith WL; Ross MA; Ionasescu R Muscle Nerve; 1996 Mar; 19(3):319-23. PubMed ID: 8606695 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]